{"orpha":730699,"name":"Genetic syndromic rhombencephalosynapsis","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-730699/","orphanet_url":"https://www.orpha.net/en/disease/detail/730699","names":{"fr":{"name":"Rhombencéphalosynapsis syndromique génétique"},"de":{"name":"Syndromale Rhombenzephalosynapsis, genetisch bedingte"},"es":{"name":"Rombencefalosinapsis sindrómica genética"},"it":{"name":"Rombencefalosinapsi sindromica genetica"},"nl":{"name":"Genetische syndromale rombencefalosynapsis"},"pt":{"name":"Genetic syndromic rhombencephalosynapsis"},"pl":{"name":"Genetic syndromic rhombencephalosynapsis"},"cs":{"name":"Genetic syndromic rhombencephalosynapsis"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":269567,"name":"Genetic syndrome with a cerebellar malformation as a major feature","classifications":[156]}],"children":[{"orpha":693549,"name":"Facial dysmorphism-Intellectual disability-rhombencephalosynapsis syndrome","type":"Malformation syndrome"},{"orpha":3412,"name":"VACTERL with hydrocephalus","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}